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Global Biobank Engine
RIVAS_HG19
About
Downloads
HLA Alleles
COVID19
Power
Sex Effects
Polygenic risk
Exomes
Array coding
Genetic correlation
DeGAs
DeGAs-Risk
snpnet-Cox
FAQ
Variant:
19:45412079 C / T
Filter Status
PASS
MAF
8.04e-02
dbSNP
rs7412
EMBL-EBI GWAS
rs7412
PhenoScanner
rs7412
UCSC
19-45412079-C-T
gnomAD
19-45412079-C-T
IBD
19-45412079-C-T
Intensity
ClinVar
Click to search for variant in Clinvar
Annotations
This variant falls on 0 transcripts in 0 genes:
missense
APOE
Transcripts
ENST00000252486 * (p.Arg176Cys)
Polyphen:
probably_damaging
; SIFT:
deleterious
ENST00000425718 (p.Arg176Cys)
Polyphen:
probably_damaging
; SIFT:
deleterious
ENST00000434152 (p.Arg202Cys)
Polyphen:
probably_damaging
; SIFT:
deleterious
ENST00000446996 (p.Arg176Cys)
Polyphen:
probably_damaging
; SIFT:
deleterious
downstream gene
APOE
-
ENST00000485628
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